Lens and Cataracts Flashcards

1
Q

the lens is a ____ structure located within the ____

A

transparent, biconvex;

posterior chamber

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2
Q

the lens is suspended in the posterior chamber via ____

A

zonules (suspensory ligaments)

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3
Q

the lens focuses ____

A

light rays to a point source on the retina

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4
Q

the lens contributes ____ of total refractive power of the eye

A

13-17 D

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5
Q

the lens has a ____ refractive index (____)

A

high; 1.3-1.4

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6
Q

the lens is composed of ____ and is divided into ____

A

epithelial cells with a basement membrane;

the embryonic nucleus, fetal nucleus, adult nucleus, cortex, and capsule

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7
Q

during gestation, a single layer of _____ forms a hollow sphere, called the _____

A

epithelial cells; lens vesicle

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8
Q

_____ cells of the lens vesicle elongate to become primary lens fibers; they fill the lens vesicle and form the ____

A

posterior;

embryonic nucleus

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9
Q

_____ cells of the lens vesicle near the equator divide to produce new epithelial cells; these cells elongate to become secondary lens fibers and form the ____, which surrounds the ____

cell elongation continues until ____; form ____, allowing cells to remain tightly connected during accommodation

as cells reach the sutures, ____; cells consist of ____

A

anterior;
fetal nucleus;
embryonic nucleus

nasal and temporal cells meet (suture); interlocking ball-and-socket and tongue-and-groove junctions

nuclei and organelles are degraded; only a cell membrane, cytoskeleton, and crystallins (proteins)

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10
Q

the anterior suture appears as ____, while the posterior suture appears as ____

A

an upright Y;

an inverted Y

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11
Q

after birth, _____ cells continue to divide and elongate;
secondary lens fibers produced after birth form the ____, which surrounds the ____

newly produced secondary lens fibers are located in the ____

new fibers continue to surround older more central fibers; growth results in concentric layers of _____;
_____ cells are removed from the lens; cells in the center of the lens are ____

A

anterior;
adult nucleus;
fetal nucleus

cortex

secondary lens fibers;
no;
the oldest cells in the body

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12
Q

the basement membrane of the outer epithelial cells is called the _____; it surrounds ____

A

lens capsule;

the entire lens

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13
Q

the lens capsule is composed of _____; arrangement makes the lens capsule ____

A

primarily type IV collagen and GAGs;

highly elastic

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14
Q

____ lens capsule thickens throughout life; lens capsule components are secreted by _____; becomes the ____ BM in the body

A

anterior;
anterior epithelial cells;
thickest

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15
Q

____ lens capsule remains the same thickness throughout life; no _____ to secrete the lens capsule components

A

posterior;

posterior epithelial cells

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16
Q

the lens absorbs _____

A

ultraviolet light

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17
Q

_____ in the lens absorb most of UV-A (320-400 nm) radiation to prevent it from _____; absorption of UV radiation leads to production of ____

A

chromophores (yellow pigment);
reaching the retina;
free radicals –> DNA damage and protein aggregation

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18
Q

the lens refracts _____

A

visible light (400-700 nm)

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19
Q

refractive power of the lens changes with ____

A

contraction of the ciliary muscle

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20
Q

What happens with contraction of the ciliary muscle?

A

zonules relax –> lens thickness increases –> lens equatorial diameter decreases –> anterior lens radius of curvature decreases (anterior surface curvature steepens) –> lens refractive power increases (> 20D) = accommodation

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21
Q

with age, ability for the lens to change its curvature is ____; ciliary body moves progressively ____; lens _____; lens rigidity ____; nucleus becomes ____ than the cortex

A
impaired (presbyopia);
inward toward the lens; 
thickens;
increases;
stiffer
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22
Q

the lens transmits ____

A

visible light (400-700 nm)

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23
Q

for optimal light transmission, the lens must be ____

A

transparent

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24
Q

the ____ are the only transparent tissues in the body

A

lens, cornea, vitreous

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25
Q

contributions to lens transparency

A
  • lack of blood vessels and nerves
  • orderly arrangement of lens fibers with uniform spacing between lens fibers; cells are hexagonal, allowing for tight, uniform packing of cells
  • few cellular organelles in the visual axis
  • high concentration of crystallins
  • Na+/K+/ATPase in epithelial cell membranes
  • presence of antioxidants glutathione and ascorbic acid (Vitamin C); neutralize free readicals
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26
Q

What are crystallins?

A

water-soluble proteins that comprise over 90% of total cellular protein; types alpha, beta, gamma;
alpha crystallins function as molecular chaperones - stabilize proteins that are partially unfolded and prevent them from aggregating;
beta and gamma crystallins have unknown functions

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27
Q

with age, the lens loses ____

A

transparency

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28
Q

with age, chromophore concentration ____;

leads to _____ and _____

A

increases;
yellowing of the lens;
DNA damage and protein aggregation

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29
Q

with age, glutathione concentration ____;

leads to _____

A

decreases;

DNA damage and protein aggregation

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30
Q

with age, alpha crystallin concentration ____;
by age 45, _____;
leads to ____

A

decreases;
no alpha crystallins evident in the lens nucleus;
protein aggregation

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31
Q

with age, epithelial cell membrane permeability ____; leading to ____

A

increases;
solutes and water enter epithelial cell –> swelling of lens fibers; disrupts orderly arrangement and uniform spacing of lens fibers

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32
Q

nuclear sclerosis

A

hardening and yellowing of the lens nucleus

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33
Q

nuclear sclerosis etiology

A

age-related

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34
Q

nuclear sclerosis demographics

A

everyone, typically begins around age 50

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35
Q

nuclear sclerosis laterality

A

bilateral > unilateral (can be asymmetric)

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36
Q

nuclear sclerosis symptoms

A
  • asymptomatic
  • blurred vision, decreased night vision
  • poor color discrimination
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37
Q

nuclear sclerosis signs

A
  • yellow lens nucleus, may progress to brown (brunescent)

- refractive shift, typically a myopic shift (“second sight”)

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38
Q

nuclear sclerosis management

A
  • monitor: 6 month to yearly observation, SL exam, grade severity
  • correct refractive error
  • refer for cataract surgery when BCVA is 20/40 or worse (most states’ legal driving requirement) or when the cataract is impacting ADLs (vision can be better than 20/40)
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39
Q

nuclear sclerosis pearls

A
  • NS can also be white or “milky”: greater effect on vision, larger myopic shift
  • slowly progressive
  • can progress to a mature or hypermature cataract
  • historically, medical insurance would only pay for surgery when the vision was 20/40 or worse
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40
Q

cortical cataract

A

opacification of the lens cortex

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41
Q

cortical cataract etiology

A

age-related

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42
Q

cortical cataract demographics

A

everyone, typically begins around age 50

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43
Q

cortical cataract laterality

A

bilateral > unilateral (can be asymmetric)

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44
Q

cortical cataract symptoms

A
  • asymptomatic
  • blurred vision
  • glare/night vision problems
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45
Q

cortical cataract signs

A
  • cortical water clefts and vacuoles in the early stages
  • spoke or wedge-like opacities in the cortex- begin in the periphery, coalesce (get thicker and larger) as the opacities encroach the visual axis
  • refractive shift, typically a hyperopic shift, lenticular cyl
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46
Q

cortical cataract management

A
  • monitor: 6 month to yearly observation, SL exam, grade severity
  • correct refractive error
  • refer for cataract surgery when BCVA is 20/40 or worse (most states’ legal driving requirement) or when the cataract is impacting ADLs (vision can be better than 20/40)
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47
Q

cortical cataract pearls

A
  • slowly progressive
  • can progress to a mature or hypermature cataract
  • often makes BIO more difficult- glare…
48
Q

mature cataract

A

complete opacification of the entire lens

49
Q

mature cataract etiology

A

progression of a cortico-nuclear cataract

50
Q

mature cataract laterality

A

bilateral > unilateral (usually have cataracts in both eyes, but only one is mature)

51
Q

mature cataract symptoms

A

significantly blurred vision (20/400, hand motion, etc.)

52
Q

mature cataract signs

A
  • complete opacification of the entire lens
  • leukocoria (white pupil)
  • shallow anterior chamber
53
Q

mature cataract complications

A

phacomorphic glaucoma

54
Q

mature cataract management

A

refer for cataract surgery

55
Q

mature cataract pearls

A
  • order B scan to evaluate posterior segment pathology

- not common where there is access to cataract surgery

56
Q

hypermature cataract (Morgagnian)

A

mature cataract with liquefaction of the cortex and sinking of the nucleus to the bottom of the lens capsule

57
Q

hypermature cataract etiology

A

progression of a mature cataract

58
Q

hypermature cataract laterality

A

bilateral or unilateral (usually only one will be hypermature)

59
Q

hypermature cataract symptoms

A

significantly blurred vision (probably not seeing much at all)

60
Q

hypermature cataract signs

A
  • complete liquefaction of the entire lens with the nucleus floating freely in the liquefied cortex
  • leukocoria
  • shallow anterior chamber
61
Q

hypermature cataract complications

A
  • lens capsule rupture
  • phacolytic uveitis
  • phacolytic glaucoma
62
Q

hypermature cataract management

A

refer for cataract surgery

63
Q

hypermature cataract pearls

A
  • order B scan to evaluate posterior segment pathology

- not common where there is access to cataract surgery

64
Q

posterior subcapsular cataract (PSC)

A

opacification between the posterior cortex and capsule

65
Q

posterior subcapsular cataract (PSC) etiology/associations

A
  • age-related
  • associated with chronic uveitis, prolonged steroid use, RP, AKC, pathological myopia, radiation, systemic disease (ex: DM, neurofibromatosis)
66
Q

posterior subcapsular cataract (PSC) demographics

A

typically begins around age 50 if age-related

67
Q

posterior subcapsular cataract (PSC) laterality

A

bilateral > unilateral

68
Q

posterior subcapsular cataract (PSC) symptoms

A
  • asymptomatic
  • blurred vision near > distance (smaller pupil size at near –> PSC fills whole visual axis; often pinhole VA will be worse)
  • glare
69
Q

posterior subcapsular cataract (PSC) signs

A
  • granular or plaque-like opacification anterior to the posterior capsule; commonly begins as a round opacity in the visual axis
  • posterior cortical opacification
70
Q

posterior subcapsular cataract (PSC) management

A
  • monitor: SL exam with retroillumination, grade severity

- cataract surgery when ADLs are affected

71
Q

posterior subcapsular cataract (PSC) pearls

A

progresses more rapidly than other senile cataracts (months vs years)*

72
Q

most common cataracts

A
  • NS
  • Cortical
  • PSC
73
Q

anterior subcapsular cataract (ASC)

A

opacification between the anterior capsule and cortex

74
Q

anterior subcapsular cataract (ASC) etiology/associations

A

associated with angle closure (cataract is termed glaucomflecken), AKC, meds (ex: phenothiazines, amiodarone), radiation

75
Q

anterior subcapsular cataract (ASC) laterality

A

bilateral > unilateral

76
Q

anterior subcapsular cataract (ASC) symptoms

A
  • asymptomatic
  • blurred vision
  • glare
77
Q

anterior subcapsular cataract (ASC) signs

A
  • granular or plaque-like opacification posterior to the anterior capsule
  • anterior cortical opacification
78
Q

anterior subcapsular cataract (ASC) management

A
  • monitor: SL exam with retroillumination, grade severity

- refer for cataract surgery when BCVA is 20/40 or worse or when the cataract is impacting ADLs

79
Q

sunflower cataract (chalcosis lentis)

A

opacification in a sunflower pattern between the anterior capsule and cortex

80
Q

sunflower cataract (chalcosis lentis) etiology/associations

A

copper deposition (Wilson disease)

81
Q

sunflower cataract (chalcosis lentis) laterality

A

bilateral > unilateral (because of association with systemic disease)

82
Q

sunflower cataract (chalcosis lentis) symptoms

A
  • asymptomatic
  • blurred vision
  • glare
83
Q

sunflower cataract (chalcosis lentis) signs

A

yellow, green, or red sunflower-like opacification beneath the anterior capsule

84
Q

sunflower cataract (chalcosis lentis) management

A
  • monitor: SL exam with retroillumination, grade severity
  • refer to PCP for evaluation of Wilson’s disease- may resolve with improvement in copper levels
  • refer for cataract surgery when BCVA is 20/40 or worse or when the cataract is impacting ADLs
85
Q

snowflake cataract

A

white opacities in the cortex

86
Q

snowflake cataract etiology/associations

A

DM

87
Q

snowflake cataract laterality

A

bilateral > unilateral

88
Q

snowflake cataract symptoms

A
  • asymptomatic
  • blurred vision
  • glare
89
Q

snowflake cataract signs

A

white, snowflake-like opacities in the cortex

90
Q

snowflake cataract management

A
  • monitor: SL exam with retroillumination, grade severity
  • refer to PCP for evaluation of DM- may resolve with improvement in BG
  • refer for cataract surgery when BCVA is 20/40 or worse or when the cataract is impacting ADLs
91
Q

snowflake cataract pearls

A

progresses rapidly

92
Q

Christmas tree cataract (polychromatic cataract)

A

glittering, multi-colored opacities in the cortex

93
Q

Christmas tree cataract (polychromatic cataract) etiology/associations

A
  • myotonic dystrophy

- rarely, age-related

94
Q

Christmas tree cataract (polychromatic cataract) laterality

A

bilateral > unilateral

95
Q

Christmas tree cataract (polychromatic cataract) symptoms

A
  • asymptomatic
  • blurred vision
  • glare
96
Q

Christmas tree cataract (polychromatic cataract) signs

A

glittering, multi-colored opacities in the cortex; evolve into typical cortical and/or subcapsular opacities often star-like in conformation

97
Q

Christmas tree cataract (polychromatic cataract) management

A
  • monitor: SL exam with retroillumination, grade severity
  • refer to PCP for evaluation of myotonic dystrophy
  • refer for cataract surgery when BCVA is 20/40 or worse or when the cataract is impacting ADLs
98
Q

the lens and diabetes mellitus

A
  • glucose increases in the aqueous as it increases in the bloodstream –> diffuses into the lens and is metabolized into sorbitol
  • refractive error can be changed as plasma glucose level changes; hyperglycemia = myopia, hypoglycemia = hyperopia
  • NS and other cataracts may develop earlier than “expected” in the patient with diabetes
99
Q

other diseases associated with cataract

A
  • myotonic dystrophy
  • atopic dermatitis
  • neurofibromatosis type 2
  • chronic anterior uveitis
  • acute angle closure
  • high myopia
  • hereditary fundus dystrophies
100
Q

traumatic cataract

A
  • the most common cause of unilateral cataract in young patients
  • penetrating trauma
  • blunt trauma
  • electric shock
  • radiation (glassblowers, etc.)
  • surgery
101
Q

cataract surgery procedure

A
  • corneal incision
  • removal of a portion of the anterior lens capsule
  • removal of the lens
  • implantation of IOL
102
Q

posterior capsular opacification (PCO)

A
  • also called “after-cataract” or “secondary cataract”

- opacification between a PCIOL and posterior capsule

103
Q

posterior capsular opacification (PCO)

A

proliferation of lens epithelial cells onto the posterior capsule

104
Q

posterior capsular opacification (PCO) laterality

A

bilateral or unilateral

105
Q

posterior capsular opacification (PCO) symptoms

A
  • asymptomatic
  • blurred vision
  • glare
106
Q

posterior capsular opacification (PCO) signs

A
  • PCIOL
  • Elschnig’s pearls (round, clear “pearls” on the posterior capsule)
  • wrinkling of the posterior capsule
107
Q

posterior capsular opacification (PCO) management

A
  • monitor: SL exam with retroillumination, grade severity

- neodymium: yttrium-aluminum-garnet (Nd: YAG) laser capsulotomy when ADLs are affected

108
Q

posterior capsular opacification (PCO) pearls

A
  • most common post-op complication of cataract surgery
  • up to 50% of patients develop PCO
  • can occur days, weeks, months, or years after surgery
109
Q

pseudoexfoliation syndrome

A

systemic disease in which grayish-white material is deposited on anterior segment structures and systemically (e.g., skin, heart, lungs)

110
Q

pseudoexfoliation syndrome etiology

A

defect in a gene; codes for an enzyme responsible for the formation of elastin fibers

111
Q

pseudoexfoliation syndrome demographics

A
  • particularly common in Scandinavians

- incidence increases after age 60 years

112
Q

pseudoexfoliation syndrome laterality

A

bilateral or unilateral

113
Q

pseudoexfoliation syndrome symptoms

A

asymptomatic

114
Q

pseudoexfoliation syndrome signs

A

grayish-white flaky deposition:

  • anterior lens capsule- central zone of deposition (often with rolled-up edges), middle clear zone, peripheral cloudy zone
  • pupillary margin
  • K endothelium
  • TM
  • anterior hyaloid
  • ciliary body
  • zonules
  • iris sphincter atrophy with TIDs at the pupillary margin
  • pigmentation of the TM, at or anterior to Schwalbe’s line (Sampaolesi line), and K endothelium
115
Q

pseudoexfoliation syndrome complications

A
  • secondary open angle glaucoma: fibrillar material and pigment may obstruct the TM
  • secondary narrow angle or angle closure glaucoma: unstable zonules can lead to anterior lens dislocation and narrow angles
  • lens (natural or implant) dislocation: zonules are unstable
116
Q

pseudoexfoliation syndrome management

A
  • monitor q6-12 months for PXF glaucoma: SL exam with retroillumination (retroillumination aids in viewing iris TIDs and lens opacities), grade severity of fibrillar deposition/pigment on anterior segment structures, ASeg photos, IOP, gonioscopy, ON photos, ON OCT, GCC, VF
  • if glaucoma develops, treatment is similar to POAG
117
Q

pseudoexfoliation syndrome pearls

A
  • pseudoexfoliation syndrome is the most common cause of secondary open angle glaucoma
  • up to 60% develop OHTN or glaucoma
  • affects 2% of US population over age 50 years